Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs2280789
LOC105371744 ; CCL5
0.925 0.080 17 35879999 intron variant A/G snv 0.16 3
rs373950030
CD209
0.882 0.080 19 7744967 missense variant C/T snv 2.0E-05 2.1E-05 3
rs386699558
LOC107986589 ; HLA-DQA1 ; HLA-DQA2
0.882 0.080 6 32642624 missense variant GCC/ACA mnv 3
rs3923647
TLR1
0.925 0.080 4 38797918 missense variant T/A;C;G snv 2.7E-02; 4.0E-06; 1.6E-05 3
rs606231248
MRC1
0.882 0.080 10 17849701 missense variant G/A snv 0.32 3
rs9272785
LOC107986589 ; HLA-DQA1 ; HLA-DQA2
0.882 0.080 6 32642624 missense variant G/A snv 0.18 8.7E-02 3
rs1135791
SP110
0.925 0.080 2 230177560 missense variant A/G snv 0.42 0.40 2
rs1194182
CD36
1.000 0.080 7 80602188 5 prime UTR variant G/C snv 0.53 2
rs12477677
LINC01857
1.000 0.080 2 207666398 intron variant T/C snv 0.22 2
rs1327474
IFNGR1
0.925 0.080 6 137219938 upstream gene variant C/T snv 0.67 2
rs1327475
IFNGR1
0.925 0.080 6 137215318 missense variant G/A snv 0.13 0.12 2
rs1371329921
TLR4
0.925 0.080 9 117712993 stop gained C/T snv 4.0E-06 1.4E-05 2
rs138968705
TLR6 ; TLR1
0.925 0.080 4 38828278 missense variant G/A snv 1.2E-04 2.3E-04 2
rs2367707
EREG
0.925 0.080 4 74382717 synonymous variant A/G snv 0.79 0.79 2
rs34069356
CTSZ
0.925 0.080 20 58995705 missense variant C/T snv 1.1E-03 4.3E-03 2
rs4331426 0.925 0.080 18 22610832 intergenic variant G/A snv 0.86 2
rs5917471
CYBB
0.925 0.080 X 37793265 intron variant C/T snv 0.55 2
rs6127698
MC3R
0.925 0.080 20 56248360 upstream gene variant G/T snv 0.39 2
rs6751745
MARCO
0.925 0.080 2 118983428 intron variant C/T snv 0.31 2
rs779826162
TLR1
0.925 0.080 4 38796574 missense variant C/T snv 2.0E-05 1.4E-05 2
rs9061
SP110 ; SP140
0.925 0.080 2 230212395 missense variant C/T snv 0.11 9.1E-02 2
rs9376267
IFNGR1
0.925 0.080 6 137209894 5 prime UTR variant C/T snv 0.22 2
rs9376268
IFNGR1
0.925 0.080 6 137211614 intron variant G/A snv 0.20 2
rs10208770
SP110
1.000 0.080 2 230170151 intron variant T/G snv 0.14 1